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Rational design reveals potent CD38 inhibitors elevate NAD+ levels in neuronal models, suggesting neuroprotection.
Cluster of differentiation 38 (CD38) is a nicotinamide adenine dinucleotide (NAD⁺)-consuming ectoenzyme abundantly expressed in brain regions involved in motor control and cognition. Given the central role of NAD⁺ in maintaining neuronal health, inhibition of CD38, resulting in NAD⁺ elevation, has emerged as a potential therapeutic approach for neurodegenerative diseases and age-associated cognitive decline. Herein, we report the rational, structure-guided optimization of a series of small-molecule CD38 inhibitors, culminating in the identification of CVN14, a potent, selective, and brain-penetrant tool molecule with favorable pharmacokinetic properties for advanced preclinical evaluation. We further disclose the first high-resolution X-ray crystal structure of the CVN14-ADPR-CD38 complex, revealing an uncompetitive binding mode. CVN14 provides a molecular tool to investigate CD38 biology in neurodegeneration and supports the development of next-generation brain-penetrant CD38 inhibitors.
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Stott et al. (2026) studied this question.
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